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Clinical Trial Summary

LCP-Tacro is an extended-release formulation of tacrolimus designed for once-daily dosing. Phase 1 studies demonstrated greater bioavailability than twice-daily tacrolimus capsules and no new safety concerns.

- Stable kidney transplant patients can be safely converted from Adoport® twice-daily to LCP-Tacro®.

- The greater bioavailability of LCP-Tacro after once-daily dosing results in similar (AUC) exposure, at a dose approximately 30% less, than the total daily dose of Adoport®.

- LCP-Tacro provides a slow drug release and this results in flatter kinetics characterized by significantly lower peak-trough fluctuations.

- CN is the major cellular target of the calcineurin inhibitors (CNIs) cyclosporine A (CsA) and tacrolimus. The ability of these drugs to inhibit CN activity is dependent on their binding to the respective immunophilins, cyclophilins A and B for CsA and FKBP12 for tacrolimus.

- CN inhibition is a rate limiting phenomenon. Over concentrations of tacrolimus does not correlate with an increase in the CN activity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02961608
Study type Interventional
Source Hospital Universitari de Bellvitge
Contact
Status Completed
Phase Phase 4
Start date May 2016
Completion date September 2018

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